Showing results (31-40 of 500) with videos related to
Sort By:
Pageof 50
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 22, 2005
Neurotoxic calcium transfer from endoplasmic reticulum to mitochondria is regulated by cyclin-dependent kinase 5-dependent phosphorylation of tauFrédéric Darios, Marie-Paule Muriel, Myriam Escobar Khondiker, et al.Comptes Rendus Biologies|March 18, 2005
Parkinson's disease: from causes to mechanismsOlga Corti, Cornelia Hampe, Frédéric Darios, et al.Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia with sensory neuropathy (SCA25)Giovanni Stevanin, Emmanuel Broussolle, Nathalie Streichenberger, et al.Genes|November 25, 2023
The Whole-Exome Sequencing of a Cohort of 19 Families with Adolescent Idiopathic Scoliosis (AIS): Candidate PathwaysLaura Marie-Hardy, Thomas Courtin, Hugues Pascal-Moussellard, et al.Journal of Neurochemistry|July 4, 2009
Atlastin-1, the dynamin-like GTPase responsible for spastic paraplegia SPG3A, remodels lipid membranes and may form tubules and vesicles in the endoplasmic reticulumMarie-Paule Muriel, Aurélien Dauphin, Michito Namekawa, et al.Neurobiology of Aging|April 16, 2013
Screening UBQLN-2 in French frontotemporal lobar degeneration and frontotemporal lobar degeneration-amyotrophic lateral sclerosis patientsSerena Lattante, Isabelle Le Ber, Agnès Camuzat, et al.Plos One|December 11, 2012
Requirement for zebrafish ataxin-7 in differentiation of photoreceptors and cerebellar neuronsConstantin Yanicostas, Elisa Barbieri, Masahiko Hibi, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|June 15, 2010
LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson's disease patientsSoraya Bardien, Angelica Marsberg, Rowena Keyser, et al.Human Molecular Genetics|November 21, 2014
Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLDSerena Lattante, Hortense de Calbiac, Isabelle Le Ber, et al.American Journal of Medical Genetics. Part A|June 9, 2005
Detection of genomic rearrangements by DHPLC: a prospective study of 90 patients with inherited peripheral neuropathies associated with 17p11.2 rearrangementsMourad Naïmi, Sandrine Tardieu, Christel Depienne, et al.Pageof 50